FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OWL CONTACT LENS CASES, DOG CONTACT LENS CASES

K Number: K130930 · Decision Feb 12, 2014
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
81
Applicant Total
1
Review Days
314

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Basic Information

Device Name
OWL CONTACT LENS CASES, DOG CONTACT LENS CASES
K Number
K130930
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5928
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ningbo Lishunda Electronics Co., Ltd.
Date Received
April 4, 2013
Decision Date
February 12, 2014
Product Code
LRX
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LRX Case, Contact Lens

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